Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_assertion description "[To clinically characterize a Swedish family with autosomal dominant retinitis pigmentosa due to a mutation, Arg-172-Trp, in the peripherin/RDS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_assertion evidence source_evidence_literature NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_assertion SIO_000772 9810570 NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_assertion wasDerivedFrom befree-20150227 NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_assertion wasGeneratedBy ECO_0000203 NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.